CA3154424A1 - Glenoid bone graft retention plate - Google Patents
Glenoid bone graft retention plate Download PDFInfo
- Publication number
- CA3154424A1 CA3154424A1 CA3154424A CA3154424A CA3154424A1 CA 3154424 A1 CA3154424 A1 CA 3154424A1 CA 3154424 A CA3154424 A CA 3154424A CA 3154424 A CA3154424 A CA 3154424A CA 3154424 A1 CA3154424 A1 CA 3154424A1
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- Prior art keywords
- retention plate
- bone graft
- plate
- recited
- suture
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 210000000988 bone and bone Anatomy 0.000 title claims abstract description 95
- 241001653121 Glenoides Species 0.000 title claims abstract description 62
- 230000014759 maintenance of location Effects 0.000 title claims abstract description 59
- 239000000463 material Substances 0.000 claims abstract description 41
- 238000000034 method Methods 0.000 claims abstract description 30
- 238000005553 drilling Methods 0.000 claims description 7
- 230000003416 augmentation Effects 0.000 claims description 4
- 230000002093 peripheral effect Effects 0.000 claims description 2
- 238000004873 anchoring Methods 0.000 claims 17
- 238000003306 harvesting Methods 0.000 claims 1
- 238000002513 implantation Methods 0.000 abstract description 10
- 230000006835 compression Effects 0.000 abstract description 9
- 238000007906 compression Methods 0.000 abstract description 9
- 229920000642 polymer Polymers 0.000 abstract description 9
- 230000006641 stabilisation Effects 0.000 abstract description 5
- 238000011105 stabilization Methods 0.000 abstract description 5
- 238000001356 surgical procedure Methods 0.000 abstract description 4
- 239000007943 implant Substances 0.000 abstract 1
- 210000004872 soft tissue Anatomy 0.000 description 7
- 210000003109 clavicle Anatomy 0.000 description 5
- 210000001991 scapula Anatomy 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- 206010065687 Bone loss Diseases 0.000 description 3
- 210000003414 extremity Anatomy 0.000 description 3
- 208000014674 injury Diseases 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000004696 Poly ether ether ketone Substances 0.000 description 2
- 208000027418 Wounds and injury Diseases 0.000 description 2
- 230000006378 damage Effects 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 239000011796 hollow space material Substances 0.000 description 2
- 210000003205 muscle Anatomy 0.000 description 2
- 229920002530 polyetherether ketone Polymers 0.000 description 2
- 230000008439 repair process Effects 0.000 description 2
- 210000000323 shoulder joint Anatomy 0.000 description 2
- 210000002435 tendon Anatomy 0.000 description 2
- 208000032984 Intraoperative Complications Diseases 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 208000035965 Postoperative Complications Diseases 0.000 description 1
- 206010057765 Procedural complication Diseases 0.000 description 1
- 229910001069 Ti alloy Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 210000004204 blood vessel Anatomy 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 210000000845 cartilage Anatomy 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 230000035876 healing Effects 0.000 description 1
- 210000002758 humerus Anatomy 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 238000009434 installation Methods 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 210000005036 nerve Anatomy 0.000 description 1
- 238000002355 open surgical procedure Methods 0.000 description 1
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- 230000007480 spreading Effects 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 239000003356 suture material Substances 0.000 description 1
- 210000002303 tibia Anatomy 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 238000002054 transplantation Methods 0.000 description 1
- 230000008733 trauma Effects 0.000 description 1
- 230000000472 traumatic effect Effects 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2/40—Joints for shoulders
- A61F2/4081—Glenoid components, e.g. cups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/28—Bones
- A61F2/2846—Support means for bone substitute or for bone graft implants, e.g. membranes or plates for covering bone defects
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/28—Bones
- A61F2/2846—Support means for bone substitute or for bone graft implants, e.g. membranes or plates for covering bone defects
- A61F2002/285—Fixation appliances for attaching bone substitute support means to underlying bone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
- A61F2002/30316—The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
- A61F2002/30329—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
- A61F2002/30461—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements sutured, ligatured or stitched
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
- A61F2002/30316—The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
- A61F2002/30329—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
- A61F2002/30476—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements locked by an additional locking mechanism
- A61F2002/30477—Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements locked by an additional locking mechanism using sharp protrusions, e.g. spikes, for anchoring into connecting prosthetic part
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/02—Prostheses implantable into the body
- A61F2/30—Joints
- A61F2002/30001—Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
- A61F2002/30316—The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
- A61F2002/30535—Special structural features of bone or joint prostheses not otherwise provided for
- A61F2002/30576—Special structural features of bone or joint prostheses not otherwise provided for with extending fixation tabs
- A61F2002/30578—Special structural features of bone or joint prostheses not otherwise provided for with extending fixation tabs having apertures, e.g. for receiving fixation screws
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2220/00—Fixations or connections for prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2220/0008—Fixation appliances for connecting prostheses to the body
- A61F2220/0016—Fixation appliances for connecting prostheses to the body with sharp anchoring protrusions, e.g. barbs, pins, spikes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2240/00—Manufacturing or designing of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
- A61F2240/001—Designing or manufacturing processes
Landscapes
- Health & Medical Sciences (AREA)
- Transplantation (AREA)
- Biomedical Technology (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Cardiology (AREA)
- Engineering & Computer Science (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Prostheses (AREA)
Abstract
A bone graft retention plate for implantation into a human glenoid and provides stabilization and compression of bony graft material is disclosed. The plate includes channels or apertures for suture or polymer retention cerclage that exhibit curved, smooth surfaces within the plate to allow the retention cerclage to pass through the plate while limiting friction and thus protecting the integrity of the retention means. The plate also includes surface features, such as spikes and posts, to provide further stabilization and implantation positioning. The plate features result in the distribution of forces across the surface area of a bone graft and achieve satisfactory compression of the bone graft against the glenoid without using fixation screws. An associated implantation technique uses a cerclage of suture or tape to bind the implant within the glenoid and may be employed in both open and arthroscopic surgical procedures.
Description
Description GLENOID BONE GRAFT RETENTION PLATE
This application claims the benefit of filing priority under 35 U.S.C. 119 5 and 37 C.F.R. 1.78 of the co-pending U.S. Provisional Application Serial No.
62/916,135 filed October 16, 2019, for a Glenoid Bone Augmentation Plate With Surgical Implantation Technique. All information disclosed in that prior filed application is incorporated herein by reference.
10 Technical Field The present invention relates generally to surgical instruments. In particular, the invention relates to stabilization plates for human bone. In greater particularity, the invention relates to shoulder socket fixation plates and related surgical installation techniques of such plates along with bone replacement 15 retention strategies.
Background Art Human shoulders can exhibit instability following trauma from injury or simply through wear. Through a traumatic event, the socket or "glenoid" of the 20 shoulder can have an injury where a piece of bone is either broken off or worn away over time. In the later circumstance, the loss of bone is an attritional process thereby providing no residual bone to reposition into the loss site.
With bone loss in the glenoid, a simple soft tissue tightening procedure results in the likelihood of recurrent instability. In response, surgeons usually replace lost bone 25 to reduce the chances of instability re-occurrence.
Various bone transfer procedures to replace lost glenoid bone are known.
Most require attaching a free piece of bone or a bone and soft-tissue combination to the targeted glenoid area. The replacement bone or bone and soft-tissue combination, referred to herein as a "graft," are typically attached with screws to 30 compress the graft replacement across the glenoid interface surface to facilitate bony healing. The types of bone graft that have been historically been utilized are an autograft coracoid, an autograft iliac crest, and an allograft distal tibia. As an alternative, an autograft distal clavicle has recently been suggested by some in the industry, but without a broad knowledgebase or well established implementation procedures.
5 The most common surgical procedure to address bone loss or glenoid fracture was pioneered by French surgeon Dr. Michel Laratjet in 1954 which uses native coracoid in combination with soft tissue attachments to not only add bone to the missing bone site, but also to use the soft tissue to reinforce the stability of the joint. This acts as a bone block which, combined with the transferred muscles 10 acting as a stmt, prevents further dislocation of the glenoid joint. The "Latarjet procedure" historically uses screw fixation to compress the coracoid bone to the native glenoid.
The Lataijet and other procedures all use screw fixation to achieve bony compression. However, using screws to compress bone replacement has several 15 disadvantages, and many intraoperative and postoperative complications result from the use of screw fixation. Screw breakage is one possible complication.
Exposure of metallic screws to the glenohumeral joint may also result in precipitous and significant cartilage wear. Furthermore, screws of longer than appropriate length may irritate the posterior glenoid soft tissue, and insertion of 20 screws may even break the graft itself. Lastly, the use of screws may require compression rates, depending upon the screw trajectory and path required to satisfactorily stabilize the graft material, that exceed the local tolerances of the bone joint structure in order to properly fix the bone graft into place, or alternatively required compression rates may simply weaken the fixation 25 arrangement necessary to achieve bony union in the graft.
A further complication in using screws is that a patient may exhibit anatomic constraints in the shoulder that may prevent ideal screw placement.
For example, the optimal placement of screws may be inhibited by tendons, nerves, and blood vessels and a surgeon may be prevented from performing a relatively 30 minor, less invasive arthroscopic procedure to augment the glenoid with bone in favor of an open surgical procedure, which results in a longer patient recovery time.
This application claims the benefit of filing priority under 35 U.S.C. 119 5 and 37 C.F.R. 1.78 of the co-pending U.S. Provisional Application Serial No.
62/916,135 filed October 16, 2019, for a Glenoid Bone Augmentation Plate With Surgical Implantation Technique. All information disclosed in that prior filed application is incorporated herein by reference.
10 Technical Field The present invention relates generally to surgical instruments. In particular, the invention relates to stabilization plates for human bone. In greater particularity, the invention relates to shoulder socket fixation plates and related surgical installation techniques of such plates along with bone replacement 15 retention strategies.
Background Art Human shoulders can exhibit instability following trauma from injury or simply through wear. Through a traumatic event, the socket or "glenoid" of the 20 shoulder can have an injury where a piece of bone is either broken off or worn away over time. In the later circumstance, the loss of bone is an attritional process thereby providing no residual bone to reposition into the loss site.
With bone loss in the glenoid, a simple soft tissue tightening procedure results in the likelihood of recurrent instability. In response, surgeons usually replace lost bone 25 to reduce the chances of instability re-occurrence.
Various bone transfer procedures to replace lost glenoid bone are known.
Most require attaching a free piece of bone or a bone and soft-tissue combination to the targeted glenoid area. The replacement bone or bone and soft-tissue combination, referred to herein as a "graft," are typically attached with screws to 30 compress the graft replacement across the glenoid interface surface to facilitate bony healing. The types of bone graft that have been historically been utilized are an autograft coracoid, an autograft iliac crest, and an allograft distal tibia. As an alternative, an autograft distal clavicle has recently been suggested by some in the industry, but without a broad knowledgebase or well established implementation procedures.
5 The most common surgical procedure to address bone loss or glenoid fracture was pioneered by French surgeon Dr. Michel Laratjet in 1954 which uses native coracoid in combination with soft tissue attachments to not only add bone to the missing bone site, but also to use the soft tissue to reinforce the stability of the joint. This acts as a bone block which, combined with the transferred muscles 10 acting as a stmt, prevents further dislocation of the glenoid joint. The "Latarjet procedure" historically uses screw fixation to compress the coracoid bone to the native glenoid.
The Lataijet and other procedures all use screw fixation to achieve bony compression. However, using screws to compress bone replacement has several 15 disadvantages, and many intraoperative and postoperative complications result from the use of screw fixation. Screw breakage is one possible complication.
Exposure of metallic screws to the glenohumeral joint may also result in precipitous and significant cartilage wear. Furthermore, screws of longer than appropriate length may irritate the posterior glenoid soft tissue, and insertion of 20 screws may even break the graft itself. Lastly, the use of screws may require compression rates, depending upon the screw trajectory and path required to satisfactorily stabilize the graft material, that exceed the local tolerances of the bone joint structure in order to properly fix the bone graft into place, or alternatively required compression rates may simply weaken the fixation 25 arrangement necessary to achieve bony union in the graft.
A further complication in using screws is that a patient may exhibit anatomic constraints in the shoulder that may prevent ideal screw placement.
For example, the optimal placement of screws may be inhibited by tendons, nerves, and blood vessels and a surgeon may be prevented from performing a relatively 30 minor, less invasive arthroscopic procedure to augment the glenoid with bone in favor of an open surgical procedure, which results in a longer patient recovery time.
2 As an alternative to screws, the medical industry has attempted to utilize fixation buttons to achieve glenoid bone fixation. However, fixation buttons often cover only a small surface area of the bone block and, generally, are not designed to allow for the free movement of suture cerclage tape or polymer 5 around the graft that is usually required for button fixation. Buttons also lack posts to control the rotation of a fixed bone block and, typically, do not afford satisfactory graft compression as compared to screw fixation techniques.
Therefore, what is needed is device and procedure to achieve bony graft fixation without the use of metallic screws or button fixation.
Disclosure of the Invention It is the object of the present invention to provide a retention plate for implantation into a human glenoid which provides stabilization and compression of two bony surfaces in conjunction with suture or polymer. The plate includes apertures for suture or polymer retention means, and smooth and countered surfaces on the plate allow the retention means to pass through while limiting friction and, thus, protecting the integrity of the retention means. The plate also includes surface features, such as spikes and posts, to provide further stabilization and implantation positioning. The plate features results in the distribution of 20 forces across the surface area of the bone graft and permits the use of suture or polymer to achieve satisfactory compression of the bone graft against the glenoid, while avoiding the use of screws for fixation. An associated implantation technique uses a cerclage of suture or tape to bind the plate within the glenoid and may be employed in both open and arthroscopic surgical procedures.
Brief Description of the Drawings An implantable retention plate incorporating the features of the invention is depicted in the attached drawings which form a portion of the disclosure and wherein:
30 Figure 1A is a sagittal view of a human left shoulder glenoid area;
Figure 1B is the view of glenoid of Fig. 1A showing the traditional use of fixation screws to fix a bone graft onto the glenoid;
Therefore, what is needed is device and procedure to achieve bony graft fixation without the use of metallic screws or button fixation.
Disclosure of the Invention It is the object of the present invention to provide a retention plate for implantation into a human glenoid which provides stabilization and compression of two bony surfaces in conjunction with suture or polymer. The plate includes apertures for suture or polymer retention means, and smooth and countered surfaces on the plate allow the retention means to pass through while limiting friction and, thus, protecting the integrity of the retention means. The plate also includes surface features, such as spikes and posts, to provide further stabilization and implantation positioning. The plate features results in the distribution of 20 forces across the surface area of the bone graft and permits the use of suture or polymer to achieve satisfactory compression of the bone graft against the glenoid, while avoiding the use of screws for fixation. An associated implantation technique uses a cerclage of suture or tape to bind the plate within the glenoid and may be employed in both open and arthroscopic surgical procedures.
Brief Description of the Drawings An implantable retention plate incorporating the features of the invention is depicted in the attached drawings which form a portion of the disclosure and wherein:
30 Figure 1A is a sagittal view of a human left shoulder glenoid area;
Figure 1B is the view of glenoid of Fig. 1A showing the traditional use of fixation screws to fix a bone graft onto the glenoid;
3 Figure 2A is a plan view of the proposed implantable retention plate;
Figure 2B is a top perspective view of the plate;
Figure 2C is a bottom perspective view of the plate;
Figure 2D is a side elevational view of the plate;
5 Figure 3A is a plan view of a second embodiment of the implantable retention plate;
Figure 313 is a top perspective view of a second embodiment of the plate;
Figure 3C is a bottom perspective view of a second embodiment of the plate;
10 Figure 3D is a side elevational view of a second embodiment of the plate;
Figure 4A is a perspective view of a procedure to extract a bone graft;
Figure 4B is a perspective view of a surgical tool holding the bone graft material;
Figure 4C is view of Fig. IA of the glenoid area showing a targeted 15 placement of the bone graft;
Figure 5A is a perspective view of a surgical tool holding the bone graft;
Figure 5B is a perspective view of the tool holding the bone graft with a drill bit positioned to create two passageways in the bone graft;
Figure 5C is a perspective view of the bone graft of Fig. 5B having the 20 plate about to be positioned on the graft;
Figure 5D is a perspective view of the bone graft combined with the plate showing the placement of the sutures relative to the plate;
Figure 6A is a human anatomical view of the glenoid with the bone graft plate combination of Fig. 5D in a targeted glenoid position;
25 Figure 6B is an isolated view of the glenoid showing a fully implanted bone graft and the retention plate in its final installed position; and, Figure 6C is an isolated view of the glenoid showing a fully implanted bone graft and a second embodiment of the retention plate in its final installed position.
Figure 2B is a top perspective view of the plate;
Figure 2C is a bottom perspective view of the plate;
Figure 2D is a side elevational view of the plate;
5 Figure 3A is a plan view of a second embodiment of the implantable retention plate;
Figure 313 is a top perspective view of a second embodiment of the plate;
Figure 3C is a bottom perspective view of a second embodiment of the plate;
10 Figure 3D is a side elevational view of a second embodiment of the plate;
Figure 4A is a perspective view of a procedure to extract a bone graft;
Figure 4B is a perspective view of a surgical tool holding the bone graft material;
Figure 4C is view of Fig. IA of the glenoid area showing a targeted 15 placement of the bone graft;
Figure 5A is a perspective view of a surgical tool holding the bone graft;
Figure 5B is a perspective view of the tool holding the bone graft with a drill bit positioned to create two passageways in the bone graft;
Figure 5C is a perspective view of the bone graft of Fig. 5B having the 20 plate about to be positioned on the graft;
Figure 5D is a perspective view of the bone graft combined with the plate showing the placement of the sutures relative to the plate;
Figure 6A is a human anatomical view of the glenoid with the bone graft plate combination of Fig. 5D in a targeted glenoid position;
25 Figure 6B is an isolated view of the glenoid showing a fully implanted bone graft and the retention plate in its final installed position; and, Figure 6C is an isolated view of the glenoid showing a fully implanted bone graft and a second embodiment of the retention plate in its final installed position.
4 Best Mode for Carrying Out the Invention Referring to the drawings for a better understanding of the function and structure of the invention, Fig. IA shows the glenoid area 10 of the body with the surrounding muscle and tendons omitted, and the humerus bone also omitted
5 The glenoid cavity 11 is circumscribed by a closed, curved periphery of scapula bone 12 onto which a margin of glenoid labrum is attached (not shown). The glenoid cavity 11 is joined to the coracoid 19 via a concave portion of scapula bone 13 and from which an example donor site of bone 16 is potentially extracted, the location of which may vary from patient to patient. The collected 10 bone from site 16 is typically transplanted in a single medical procedure onto a worn or damaged glenoid cavity periphery 14 to form a graft 15 that buttresses the glenoid. A lower portion of the scapula 17 supports both the glenoid cavity 11, the coracoid 19, and the newly transplanted graft.
Fig. 1B shows a traditional fixation method for the glenoid area 10 in 15 which the bone collected from the extraction donor site 22 is positioned onto the worn site 14 as a graft 21. One or more fixation screws 23 penetrate the graft and the supporting scapula bone 17 below the glenoid cavity surface as shown to hold the graft in place.
Figs. 2A-2D show different views of one embodiment of the invention.
20 Implantable plate 30 includes a top surface 38 having a generally rectangular shape with curved outer sidewall 51 depending downward from top surface 38.
Plate body 32 will typically have a length x (39) of approximately 15mm-20mm and a width y (41) of approximately lOmm, but as may be understood plates of various lengths x and widths y would be sized to accommodate a wide range of 25 patient glenoid shapes and sizes. Body 32 includes a recessed circular portion 34 formed in surface 38 which is bisected by recessed slot 33 connecting a pair of circular passageways 46,46.' Recess 34 allows for the use of a surgical temp or a plate holder (not shown) to assist in the positioning of the plate 30 during implantation. Body 32 may be made of any suitably ridged material to support 30 bone graft compression and fixation, such as, for example, aluminum, stainless steel, high grade polymer, titanium, titanium alloy, PEEK (poly-ether-ether ketone), etc., as long as the material used is suitable for long-term implantation within a human body. Slot 33 and passageways 46,46' are formed as an interior, integral hollow space 44 with each passageway 46,46' providing an opening or aperture from the top surface 38 to lower surface 35 and extending through lower openings 47,47', which depend downward from lower surface 35 to form two positioning posts. A pair of small suture holes 42,42' are positioned toward left and right peripheral margins of body 32 and provide angled, suture fixation points from top surface 38 to the sides 36 of body 32, and supply supplemental fixation points during a medical procedure. A plurality of sharp points or spikes 49 extend downward from lower surface 35 by a distance of approximately 3mm and are positioned to provide provisional gripping to an adjacent bone graft. The present embodiment utilizes 6 spikes, but as may be understood the number and positioning of the spikes 49 will vary with the size and configuration of the plate 30 responsive to a patients glenoid size and shape. The two passageways 46,46' are spaced apart approximately lOmm and together with integral hollow space 44 are arranged to allow for positioning control of plate 30 during implantation against g,lenoid cavity 11 with sutures. As shown, the passageways 46,46' and slot 33 are integrally curved, avoiding any sharp turns, to facilitate the distribution of downward force applied to the bone graft material by a fixation suture in a nonbinding or slidable manner.
A second embodiment of the invention may be seen in Figs. 3A-3D.
Body 32 has dimensions similar to the plate shown in Fig. 2A and also has a generally rectangular body 32 as before. However, second embodiment 60 includes a central recessed portion 71 formed in body 32, having a lowered uniform surface 72 that defines a central passageway 73, instead of an integral slot connecting two passageways as in embodiment 30.
Central passageway 73 is bisected into a two opposing channels or passageways starting at a smooth, downwardly curved median 66 extending from recessed surface 72 through to lower portion 67. A pair of alternative suture passageways 65,65' are centrally disposed on surface 38 and positioned in line with the two exterior small suture apertures 31,31' and central passageway 73, and extend through body 32 from upper surface 38 to lower surface 35. The upper portion of passageways 65,65' are chamfered at their juncture with upper surface 38 to allow for the optional use
Fig. 1B shows a traditional fixation method for the glenoid area 10 in 15 which the bone collected from the extraction donor site 22 is positioned onto the worn site 14 as a graft 21. One or more fixation screws 23 penetrate the graft and the supporting scapula bone 17 below the glenoid cavity surface as shown to hold the graft in place.
Figs. 2A-2D show different views of one embodiment of the invention.
20 Implantable plate 30 includes a top surface 38 having a generally rectangular shape with curved outer sidewall 51 depending downward from top surface 38.
Plate body 32 will typically have a length x (39) of approximately 15mm-20mm and a width y (41) of approximately lOmm, but as may be understood plates of various lengths x and widths y would be sized to accommodate a wide range of 25 patient glenoid shapes and sizes. Body 32 includes a recessed circular portion 34 formed in surface 38 which is bisected by recessed slot 33 connecting a pair of circular passageways 46,46.' Recess 34 allows for the use of a surgical temp or a plate holder (not shown) to assist in the positioning of the plate 30 during implantation. Body 32 may be made of any suitably ridged material to support 30 bone graft compression and fixation, such as, for example, aluminum, stainless steel, high grade polymer, titanium, titanium alloy, PEEK (poly-ether-ether ketone), etc., as long as the material used is suitable for long-term implantation within a human body. Slot 33 and passageways 46,46' are formed as an interior, integral hollow space 44 with each passageway 46,46' providing an opening or aperture from the top surface 38 to lower surface 35 and extending through lower openings 47,47', which depend downward from lower surface 35 to form two positioning posts. A pair of small suture holes 42,42' are positioned toward left and right peripheral margins of body 32 and provide angled, suture fixation points from top surface 38 to the sides 36 of body 32, and supply supplemental fixation points during a medical procedure. A plurality of sharp points or spikes 49 extend downward from lower surface 35 by a distance of approximately 3mm and are positioned to provide provisional gripping to an adjacent bone graft. The present embodiment utilizes 6 spikes, but as may be understood the number and positioning of the spikes 49 will vary with the size and configuration of the plate 30 responsive to a patients glenoid size and shape. The two passageways 46,46' are spaced apart approximately lOmm and together with integral hollow space 44 are arranged to allow for positioning control of plate 30 during implantation against g,lenoid cavity 11 with sutures. As shown, the passageways 46,46' and slot 33 are integrally curved, avoiding any sharp turns, to facilitate the distribution of downward force applied to the bone graft material by a fixation suture in a nonbinding or slidable manner.
A second embodiment of the invention may be seen in Figs. 3A-3D.
Body 32 has dimensions similar to the plate shown in Fig. 2A and also has a generally rectangular body 32 as before. However, second embodiment 60 includes a central recessed portion 71 formed in body 32, having a lowered uniform surface 72 that defines a central passageway 73, instead of an integral slot connecting two passageways as in embodiment 30.
Central passageway 73 is bisected into a two opposing channels or passageways starting at a smooth, downwardly curved median 66 extending from recessed surface 72 through to lower portion 67. A pair of alternative suture passageways 65,65' are centrally disposed on surface 38 and positioned in line with the two exterior small suture apertures 31,31' and central passageway 73, and extend through body 32 from upper surface 38 to lower surface 35. The upper portion of passageways 65,65' are chamfered at their juncture with upper surface 38 to allow for the optional use
6 of fixation screws (not shown) to be used in passageways 65,65' in a manner that results in the tops of each screw to be flush with or below surface 38.
Referring now to Figs. 4A-4C and Figs. 5A-5D, a series of steps are shown to illustrate extraction of bone material and preparation of that material 5 for use with the retention plate 30 shown in Fig. 2A. As will be understood, the steps shown can be adapted to be used with plate 60 shown in Fig. 3A. As seen in Fig. 4A, bone graft material may be harvested in a standard manner using standard techniques and may be obtained from the distal clavicle 80, from the coracoid area shown in Fig. 1A, or from other suitable donor sites in the patient's 10 body. A transverse or longitudinal incision 82 is made over a the clavicle region 87 of the patient, spreaders 81,81' used to enlarge the opening, and the deltotrapezial layer 88 exposed. The acromioclavicular capsule is then incised and the distal clavicle cut with a surgical saw and an osteotome 83 having a sharp, beveled tip 84 (101 in Fig. 4B) used to collect bone graft material.
15 Typically, bone material 102 is a minimum of 20mm superior to inferior, 10mm medial to lateral, and lOmm anterior to posterior, as shown 100. The amount and density of the material 102 must comport with the target site 14a so that the repair or augmentation goals of the glenoid are 11 satisfied.
After the graft material 102 is obtained, a bone clamp 115 is used to 20 stabilize 110 the graft material 112 for additional preparation. The clamp 115 includes on each side 111,111' a pair of opposing apertures 113 sized for the passage of an appropriate drilling bit 116. The clamp 115 is used to compact and form the material 112 into the size and shape needed, and one or two holes drilled 117 through the material a suitable distance apart from each other to match the 25 passageways present in a selected retention plate. Typically, a single hole is drilled for small grafts while two holes are drilled for standard sized grafts. As shown in Fig. 5C, the retention plate 30, for example, is pressed 130 onto the formed bone graft material 131 such that the passageways 46,46' are aligned with and engaged within the drilled holes 117 starting with lower post portions 47,47' 30 that assist with positioning. Once fully engaged, a shuttling loop 141 (Fig. 5D) is placed from deep to superficial in one hole and superficial to deep in the other
Referring now to Figs. 4A-4C and Figs. 5A-5D, a series of steps are shown to illustrate extraction of bone material and preparation of that material 5 for use with the retention plate 30 shown in Fig. 2A. As will be understood, the steps shown can be adapted to be used with plate 60 shown in Fig. 3A. As seen in Fig. 4A, bone graft material may be harvested in a standard manner using standard techniques and may be obtained from the distal clavicle 80, from the coracoid area shown in Fig. 1A, or from other suitable donor sites in the patient's 10 body. A transverse or longitudinal incision 82 is made over a the clavicle region 87 of the patient, spreaders 81,81' used to enlarge the opening, and the deltotrapezial layer 88 exposed. The acromioclavicular capsule is then incised and the distal clavicle cut with a surgical saw and an osteotome 83 having a sharp, beveled tip 84 (101 in Fig. 4B) used to collect bone graft material.
15 Typically, bone material 102 is a minimum of 20mm superior to inferior, 10mm medial to lateral, and lOmm anterior to posterior, as shown 100. The amount and density of the material 102 must comport with the target site 14a so that the repair or augmentation goals of the glenoid are 11 satisfied.
After the graft material 102 is obtained, a bone clamp 115 is used to 20 stabilize 110 the graft material 112 for additional preparation. The clamp 115 includes on each side 111,111' a pair of opposing apertures 113 sized for the passage of an appropriate drilling bit 116. The clamp 115 is used to compact and form the material 112 into the size and shape needed, and one or two holes drilled 117 through the material a suitable distance apart from each other to match the 25 passageways present in a selected retention plate. Typically, a single hole is drilled for small grafts while two holes are drilled for standard sized grafts. As shown in Fig. 5C, the retention plate 30, for example, is pressed 130 onto the formed bone graft material 131 such that the passageways 46,46' are aligned with and engaged within the drilled holes 117 starting with lower post portions 47,47' 30 that assist with positioning. Once fully engaged, a shuttling loop 141 (Fig. 5D) is placed from deep to superficial in one hole and superficial to deep in the other
7 hole 142. An additional suture may be placed through the inferior drill holes 42,42' (See Figs. 2A-2B) as a traction suture (not shown).
Referring now to Fig. 6A-6B, an open or arthroscopic procedure is used after the bone graft material 131 and retention plate 30 are prepared to administer the graft combination 140 to the targeted glenoid site 15.
For example, arthroscopic portals may be created to enter the glenohumeral joint 160 so that in an augmentation requirement due to anterior glenoid bone loss is confirmed, followed by biologic preparation to receive the bone graft/retention plate combination 140. A spinal needle or other rigid instrument is used to access the trajectory of the drill tunnels 141 and an incision made with blunt spreading through the deltoid 164 and infraspinatus tissue 172. Contact with the posterior glenoid 165 may then be done. A cannulated drill guide is introduced posteriorly and used to drill two parallel holes 141 to the desired location target location 15.
A k-wire 171 is placed into position and then a cannulated drill is placed over the wire and repeated for the second drill hole 141.
A shuttling suture is then placed through the cannulated drill holes and pulled through the anterior glenoid 166. The cannulated drill guide is removed and the ends of the sutures are secured. The two drill holes 141 are assessed by viewing from an anterior viewing portal to make sure that there is at least 5mm of bone present between both of the two drill holes and the face of the glenoid 162.
After satisfactory placement, a camera is placed posteriorly again, and the suture strands are used to pull suture tape or polymer through passages 46,46' of the plate 30 in a cerclage arrangement for fixation of the retention plate 30 and graft material 131 combination against the anterior glenoid 166. Each suture in the glenoid 12 is pulled, thereby pulling the two ends of the suture tape or polymer around the combination 140. Using a single traction suture, the combination is then pulled through the anterior soft tissue cannula into the joint, and the two limbs of the single cerclage suture tape or polymer pulled to remove any slack or extraneous suture material. Once the bone graft is positioned next to the native glenoid, traction is applied to the ends of the sutures to allow for proper bone contact, and a suture tape tensioning device advanced from the posterior incision such that both ends of the single limb of suture are placed into the tensioning
Referring now to Fig. 6A-6B, an open or arthroscopic procedure is used after the bone graft material 131 and retention plate 30 are prepared to administer the graft combination 140 to the targeted glenoid site 15.
For example, arthroscopic portals may be created to enter the glenohumeral joint 160 so that in an augmentation requirement due to anterior glenoid bone loss is confirmed, followed by biologic preparation to receive the bone graft/retention plate combination 140. A spinal needle or other rigid instrument is used to access the trajectory of the drill tunnels 141 and an incision made with blunt spreading through the deltoid 164 and infraspinatus tissue 172. Contact with the posterior glenoid 165 may then be done. A cannulated drill guide is introduced posteriorly and used to drill two parallel holes 141 to the desired location target location 15.
A k-wire 171 is placed into position and then a cannulated drill is placed over the wire and repeated for the second drill hole 141.
A shuttling suture is then placed through the cannulated drill holes and pulled through the anterior glenoid 166. The cannulated drill guide is removed and the ends of the sutures are secured. The two drill holes 141 are assessed by viewing from an anterior viewing portal to make sure that there is at least 5mm of bone present between both of the two drill holes and the face of the glenoid 162.
After satisfactory placement, a camera is placed posteriorly again, and the suture strands are used to pull suture tape or polymer through passages 46,46' of the plate 30 in a cerclage arrangement for fixation of the retention plate 30 and graft material 131 combination against the anterior glenoid 166. Each suture in the glenoid 12 is pulled, thereby pulling the two ends of the suture tape or polymer around the combination 140. Using a single traction suture, the combination is then pulled through the anterior soft tissue cannula into the joint, and the two limbs of the single cerclage suture tape or polymer pulled to remove any slack or extraneous suture material. Once the bone graft is positioned next to the native glenoid, traction is applied to the ends of the sutures to allow for proper bone contact, and a suture tape tensioning device advanced from the posterior incision such that both ends of the single limb of suture are placed into the tensioning
8
9 device. The two limbs of the suture are then fed into each other or spliced to allow for fixation, and the tensioning device engaged with direct visualization from the anterior portal. Once final tightening is done, the posterior suture is tied 161 and a probe used to assess the stability of the arrangement. Additional anterior labral repair may be performed superior and inferior to the retention plate/bone graft combination 140 in a standard fashion. Fig. 6B shows how the final arrangement should appear. Fig. 6C shows how a final arrangement using the above described procedure will appear using the retention plate 60 shown in Fig. 3A. As shown, a fixation button 173 may be utilized to secure the suture tape through passageway 183.
While I have shown my invention in one form, it will be obvious to those skilled in the an that it is not so limited but is susceptible of various changes and modifications without departing from the spirit thereof For example, the invention may be employed in various techniques to achieve reconstruction goals in which bone graft material must be fixed in place within a human body. For example, the invention may be used for bone block transplantation, such as in Latarjet procedures, iliac crest transfers, distal clavicle transfers, allograft transfers, bone fusions, osteotomies, and fracture fixation procedures. The invention may generally be utilized for small joint surgeries as well. The inventors further contemplate that the herein described devices and procedures may be applied to mammals of various types, in addition to human patients.
While I have shown my invention in one form, it will be obvious to those skilled in the an that it is not so limited but is susceptible of various changes and modifications without departing from the spirit thereof For example, the invention may be employed in various techniques to achieve reconstruction goals in which bone graft material must be fixed in place within a human body. For example, the invention may be used for bone block transplantation, such as in Latarjet procedures, iliac crest transfers, distal clavicle transfers, allograft transfers, bone fusions, osteotomies, and fracture fixation procedures. The invention may generally be utilized for small joint surgeries as well. The inventors further contemplate that the herein described devices and procedures may be applied to mammals of various types, in addition to human patients.
Claims (23)
1. A bone graft retention plate for compressing bone graft material against a target glenoid area, comprising:
a. a rigid plate body having an upper and lower surface, said body having a generally rectangular shape;
b. a recessed portion in said upper surface defining a suture anchoring path disposed generally within the center of said plate body, wherein said anchoring path includes two separate downward descending passageways extending from said upper surface to said lower surface;
c. wherein said two downward descending passageways form in said lower surface at least one post depending downward from said lower surface for positioning said plate onto said bone graft material; and, d+ an anchoring suture positioned through said two anchoring paths and adapted to form a cerclage around a portion of human bone for securing said retention plate and bone graft material against said glenoid area.
a. a rigid plate body having an upper and lower surface, said body having a generally rectangular shape;
b. a recessed portion in said upper surface defining a suture anchoring path disposed generally within the center of said plate body, wherein said anchoring path includes two separate downward descending passageways extending from said upper surface to said lower surface;
c. wherein said two downward descending passageways form in said lower surface at least one post depending downward from said lower surface for positioning said plate onto said bone graft material; and, d+ an anchoring suture positioned through said two anchoring paths and adapted to form a cerclage around a portion of human bone for securing said retention plate and bone graft material against said glenoid area.
2. The retention plate as recited in claim 1, wherein said two downward descending suture passageways present solely smooth curved surfaces to said suture positioned therein such that said anchoring suture slides freely within said retention plate.
3. The retention plate as recited in claim 2, further comprising a plurality of spikes depending downward from said lower surface for provisional retention of said bone graft material against said retention plate.
4. The retention plate as recited in claim 3, wherein said body further defines at least two apertures each adapted for receiving a fixation screw through said upper surface and extending through said body, wherein each screw is adapted for anchoring said retention plate against said glenoid
5. The retention plate as recited in claim 1, wherein said two descending suture passageways comprise a single central aperture in said body having a median divider extending through the center of said central aperture to form two suture channels.
6. The retention plate as recited in claim 5, wherein said two downward descending suture passageways present solely smooth curved surfaces to said suture positioned therein such that said anchoring suture slides freely within said retention plate.
7. The retention plate as recited in claim 6, further comprising a plurality of spikes depending downward from said lower surface for provisional retention of said bone graft material against said retention plate.
8. The retention plate as recited in claim 1, wherein said two descending suture passageways comprise a pair of apertures formed in and extending between said upper and lower surfaces, wherein said pair of apertures are connected within said plate body via a slot recessed in said upper surface.
9. The retention plate as recited in claim 8, wherein said pair of apertures depending downward from said lower surface form two depending posts for positioning said plate onto said bone graft material.
10. The retention plate as recited in claim 9, further comprising a plurality of spikes depending downward from said lower surface for provisional retention of said bone graft material against said retention plate.
11. The retention plate as recited in claim 10, further including upstanding side walls connecting said upper and lower surfaces, wherein said upper surface and side walls define a least two suture apertures connecting said upper surface and said side walls at the peripheral margin of said upper surface.
12. A bone graft retention plate, comprising:
a. a rigid plate body having upper and lower surfaces and bounded by generally perpendicular sides;
b. a pair of smooth walled anchor passageways disposed within said plate body and connecting said upper and lower surfaces, said passageways including lower portions depending downward from said lower surface to form at least one hollow positioning post;
c. a closed loop anchoring suture positioned within said passageways and configured to form a cerclage within a portion of glenoid bone;
d. wherein said passageways are configured to reduce friction of said anchoring suture when pulled therethrough; and, e. a plurality of spikes depending downward from said lower body surface for provisional fixation against a shaped mass of glenoid suitable bone graft material.
a. a rigid plate body having upper and lower surfaces and bounded by generally perpendicular sides;
b. a pair of smooth walled anchor passageways disposed within said plate body and connecting said upper and lower surfaces, said passageways including lower portions depending downward from said lower surface to form at least one hollow positioning post;
c. a closed loop anchoring suture positioned within said passageways and configured to form a cerclage within a portion of glenoid bone;
d. wherein said passageways are configured to reduce friction of said anchoring suture when pulled therethrough; and, e. a plurality of spikes depending downward from said lower body surface for provisional fixation against a shaped mass of glenoid suitable bone graft material.
13. The retention plate as recited in claim 12, wherein said two anchoring passageways comprise a single central aperture in said body having a median divider extending through the center of said central aperture to form two suture channels.
14. The retention plate as recited in claim 13, wherein said two anchoring passageways are adapted to permit said anchoring suture to slide freely withing said passageways.
15. The retention plate as recited in claim 12, wherein said two anchoring passageways comprise a pair of apertures formed in and extending between said upper and lower surfaces, wherein said pair of apertures are connected within said plate body via a slot recessed in said upper surface.
16. The retention plate as recited in claim 15, wherein said pair of apertures depending downward from said lower surface form two depending posts for positioning said plate onto said bone graft material.
17. The retention plate as recited in claim 16, further comprising a plurality of spikes depending downward from said lower surface for provisional retention of said bone graft material against said retention plate.
18. A procedure for fixing a shaped mass of glenoid suitable bone graft material to augment the glenoid area of a human body, comprising the steps of:
a. obtaining suitable amount of bone graft material to augment said targeted glenoid area;
b+ compressing said bone graft material with a bone clamp;
c. pressing the compressed bone graft material against the retention plate recited in claim 1;
d. drilling at least one aperture through said bone graft material aligned with two descending passageways in the retention plate;
e. positioning the combination bone graft material and retention plate on a targeted glenoid augmentation area through a medical procedure; and, f. drilling at least one tunnel through bone supporting said targeted glenoid area and threading an anchoring suture through said combination bone graft material and retention plate in a cerclage arrangement such that said combination of bone graft material and retention plate are compressed against said targeted glenoid area.
a. obtaining suitable amount of bone graft material to augment said targeted glenoid area;
b+ compressing said bone graft material with a bone clamp;
c. pressing the compressed bone graft material against the retention plate recited in claim 1;
d. drilling at least one aperture through said bone graft material aligned with two descending passageways in the retention plate;
e. positioning the combination bone graft material and retention plate on a targeted glenoid augmentation area through a medical procedure; and, f. drilling at least one tunnel through bone supporting said targeted glenoid area and threading an anchoring suture through said combination bone graft material and retention plate in a cerclage arrangement such that said combination of bone graft material and retention plate are compressed against said targeted glenoid area.
19. The procedure as recited in claim 18, wherein said step of drilling at least one tunnel through bone supporting said glenoid area comprises drilling two tunnels, and wherein each tunnel receives an anchoring suture in said cerclage arrangement.
20. The procedure as recited in claim 19, wherein said step of obtaining suitable bone graft material comprises the step of harvesting donor bone material from said same human body.
21. The procedure as recited in claim 20, further including the step of using an anchoring buuon in said cerclage arrangement positioned on said bone supporting said glenoid area.
22. The procedure as recited in claim 18, wherein said step of drilling at least one aperture through said bone graft material comprising drilling a plurality of apertures, each aperture aligned with a unique passageway present in said retention plate
23. The procedure as recited in claim 22, further including the step of using an anchoring button in said cerclage arrangement positioned on said bone supporting said glenoid area.
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US62/916,135 | 2019-10-16 | ||
PCT/US2020/048541 WO2021080689A1 (en) | 2019-10-16 | 2020-08-28 | Glenoid bone graft retention plate |
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US722944A (en) | 1902-04-23 | 1903-03-17 | Paul Henri Joseph Chautard | Process of devulcanizing gums. |
US6224602B1 (en) | 1999-10-11 | 2001-05-01 | Interpore Cross International | Bone stabilization plate with a secured-locking mechanism for cervical fixation |
FR2800268B1 (en) * | 1999-10-29 | 2002-04-19 | Topline Technology Llc | ORTHOPEDIC SUTURE AND ANCILLARY PLATE FOR THE PLACEMENT OF SUCH A PLATE |
US7887551B2 (en) * | 1999-12-02 | 2011-02-15 | Smith & Nephew, Inc. | Soft tissue attachment and repair |
ATE503442T1 (en) * | 2004-05-19 | 2011-04-15 | Zimmer Gmbh | GLENOID ANCHORAGE |
US7229444B2 (en) * | 2004-08-25 | 2007-06-12 | Howmedica Osteonics Corp. | Trochanteric cerclage plate |
US7604657B2 (en) * | 2005-09-19 | 2009-10-20 | Depuy Products, Inc. | Bone fixation plate with complex suture anchor locations |
EP2135562B1 (en) * | 2008-06-20 | 2015-09-09 | Arthrex, Inc. | Wedged profile plate |
US8926661B2 (en) * | 2011-06-02 | 2015-01-06 | Smith & Nephew, Inc. | Surgical fastening |
EP2630935B1 (en) * | 2012-02-27 | 2014-12-31 | Arthrex, Inc. | Glenoid extension block |
US20160270922A1 (en) | 2015-03-19 | 2016-09-22 | Limacorporate S.P.A. | Glenoid Anchor for a Shoulder Joint Prosthesis |
AU2017326464B2 (en) * | 2016-09-18 | 2021-08-12 | Harry B. Skinner | Tactile cerclage wire and cable passer and methods of use |
EP3515367A1 (en) * | 2016-09-19 | 2019-07-31 | Smith & Nephew, Inc | Glenoid implant and method of use thereof |
WO2019049074A1 (en) * | 2017-09-11 | 2019-03-14 | DePuy Synthes Products, Inc. | Plug in struts for graft cage |
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EP4044945A1 (en) | 2022-08-24 |
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